(Q52548936)

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Towards a unifying mechanism for CYP17 mutations that cause isolated 17,20-lyase deficiency.

scientific article published in November 2002

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Europe PubMed Central

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12530647

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3 May 2018

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http://europepmc.org/abstract/MED/12530647

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Towards a unifying mechanism for CYP17 mutations that cause isolated 17,20-lyase deficiency. (English)

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12530647

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3 May 2018

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author name string

Richard J Auchus

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1

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12530647

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Manisha K Gupta

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2

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1 November 2002

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published in

Endocrine Research

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volume

28

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4

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443-447

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cites work

Improved method for high efficiency transformation of intact yeast cells

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Crossref

reference URL

https://api.crossref.org/works/10.1081%2FERC-120016821

retrieved

21 January 2018

Cytochrome b5 augments the 17,20-lyase activity of human P450c17 without direct electron transfer

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https://api.crossref.org/works/10.1081%2FERC-120016821

retrieved

21 January 2018

The genetic and functional basis of isolated 17,20-lyase deficiency

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https://api.crossref.org/works/10.1081%2FERC-120016821

retrieved

21 January 2018

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DOI

10.1081/ERC-120016821

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12530647

retrieved

3 May 2018

reference URL

http://europepmc.org/abstract/MED/12530647

PubMed publication ID

12530647

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12530647

retrieved

3 May 2018

reference URL

http://europepmc.org/abstract/MED/12530647

(Q52548936)

Towards a unifying mechanism for CYP17 mutations that cause isolated 17,20-lyase deficiency.

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